Canonical Allele Identifier: PA2825920338
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 393389
ClinVar RCV Id: RCV000445535 RCV001861647 RCV003126740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Met623Lys
CA16609252
NM_001145853.1:c.1868T>A