Canonical Allele Identifier: PA2741923565
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2794872
ClinVar RCV Id: RCV003675090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Phe516Leu
CA356175902
NM_006005.3:c.1546T>C
CA356175911
NM_006005.3:c.1548C>A
CA356175913
NM_006005.3:c.1548C>G