Original source

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

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

Chromosome 14:23428583 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM992933 ; PhenCode FHC0131 (C/T)

Most severe consequence
Synonyms

Uniprot VAR_020806

This variation has 6 HGVS names - click the plus to show

Variation displays