Canonical Allele Identifier: PA2825920731
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1391404
ClinVar RCV Id: RCV001893060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ser855Leu
CA2839781
NM_001145853.1:c.2564C>T
CA2573138345
NM_001145853.1:c.2564_2565delinsTG