Canonical Allele Identifier: PA645395739
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 349316

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Asp367Asn
CA10618995
NM_006005.3:c.1099G>A