Canonical Allele Identifier: PA2825920446
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 427196
ClinVar RCV Id: RCV000490103
ClinVar Variation Id: 2429743
ClinVar RCV Id: RCV003127196

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Gln687His
CA2839587
NM_001145853.1:c.2061G>C
CA356177623
NM_001145853.1:c.2061G>T