Canonical Allele Identifier: PA105725
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4512
ClinVar RCV Id: RCV000004770 RCV001387727 RCV002243622 RCV002496259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Pro504Leu
CA253190
NM_001145853.1:c.1511C>T