Allele Registry

Canonical Allele Identifier: PA105482

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000730495

ClinVar Variation:

516852

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139325.1:p.Ala58Val	CA2838811 NM_001145853.1:c.173C>T