Original source

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

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

Chromosome 19:17983405 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981845

Most severe consequence
Clinical significance

Synonyms

LSDB 10650

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

19:g.17983405G>C
ENST00000222248.3:c.277G>C
ENSP00000222248.2:p.Gly93Arg

Variation displays