Canonical Allele Identifier: PA645395712
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 393386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Pro216Arg
CA2838986
NM_006005.3:c.647C>G