Canonical Allele Identifier: PA645395755
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 393388
ClinVar RCV Id: RCV000445460 RCV000993556 RCV001157339 RCV001157340 RCV002509384 RCV000825498
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Ala422Val
CA2839291
NM_006005.3:c.1265C>T