Canonical Allele Identifier: PA2741923894
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2814578
ClinVar RCV Id: RCV003682986

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Asn849Thr
CA356179183
NM_006005.3:c.2546A>C