Canonical Allele Identifier: PA645395684
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 349302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Pro10Ser
CA2838778
NM_006005.3:c.28C>T