Canonical Allele Identifier: PA2825920276
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1407986
ClinVar RCV Id: RCV001909744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Trp588Cys
CA2839480
NM_001145853.1:c.1764G>T
CA356176783
NM_001145853.1:c.1764G>C