Canonical Allele Identifier: PA2825920384
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 178597
ClinVar RCV Id: RCV000155347 RCV000767006 RCV000515318 RCV000677339 RCV001152091 RCV004534992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Arg653Cys
CA295791
NM_001145853.1:c.1957C>T