Canonical Allele Identifier: PA2825919684
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1317454
ClinVar RCV Id: RCV001768020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Lys221Asn
CA356172258
NM_001145853.1:c.663G>C
CA356172259
NM_001145853.1:c.663G>T