Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 10:73544808 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM057323

Most severe consequence
Clinical significance

Synonyms

LSDB 13252

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

10:g.73544808T>C
ENST00000224721.6:c.5678T>C
ENSP00000224721.6:p.Phe1893Ser

Variation displays