Canonical Allele Identifier: PA645395770
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 425325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Pro504Thr
CA16621815
NM_006005.3:c.1510C>A