Original source

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

Alleles
A/G/T | Ancestral: A | Ambiguity code: D
Location

Chromosome 17:41276061 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM004187, CM012906

Most severe consequence
Clinical significance

Synonyms

LSDB U14680.1:c.53T>A, U14680.1:c.53T>C

This variation has 92 HGVS names - click the plus to show

Variation displays