Canonical Allele Identifier: PA2580317291
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2134530
ClinVar RCV Id: RCV003058141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.His401Tyr
CA356174452
NM_006005.3:c.1201C>T