Canonical Allele Identifier: PA2825920764
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1450057
ClinVar RCV Id: RCV001989950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Val871Leu
CA356179472
NM_001145853.1:c.2611G>C
CA356179475
NM_001145853.1:c.2611G>T