Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 6:121768574 (forward strand) | View in location tab

Co-located

with COSMIC COSM320581 (A/T) ; HGMD-PUBLIC CM050267

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 1381, 2010_April_001_068_GJA1_121014_0013

This variation has 3 HGVS names - click the plus to show

6:g.121768574A>C
ENST00000282561.3:c.581A>C
ENSP00000282561.3:p.His194Pro

Variation displays