Canonical Allele Identifier: PA2741923629
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2794567
ClinVar RCV Id: RCV003672922

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Ala616Pro
CA356176952
NM_006005.3:c.1846G>C