Canonical Allele Identifier: PA2825919973
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215387

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Val412Ala
CA322524
NM_001145853.1:c.1235T>C