Canonical Allele Identifier: PA2825920300
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2075914
ClinVar RCV Id: RCV002979015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Val601Leu
CA2839499
NM_001145853.1:c.1801G>T
CA356176870
NM_001145853.1:c.1801G>C