Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 6:73615425 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM993213

Most severe consequence
Clinical significance

Synonyms

LSDB 12595

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

6:g.73615425G>C
ENST00000355773.5:c.1001C>G
ENSP00000348019.5:p.Pro334Arg

Variation displays