Canonical Allele Identifier: PA2825920166
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 450291
ClinVar RCV Id: RCV000523871 RCV003126790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Phe524Leu
CA356176020
NM_001145853.1:c.1570T>C
CA356176028
NM_001145853.1:c.1572C>A
CA356176030
NM_001145853.1:c.1572C>G