Canonical Allele Identifier: PA2825919801
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1298954
ClinVar RCV Id: RCV001727284

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Trp314Arg
CA356173926
NM_001145853.1:c.940T>A
CA356173927
NM_001145853.1:c.940T>C