Canonical Allele Identifier: PA658812787
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 504707
ClinVar RCV Id: RCV000612750 RCV002532737 RCV002509080 RCV004530733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Phe264Leu
CA2839056
NM_006005.3:c.792C>G
CA356172548
NM_006005.3:c.790T>C
CA356172551
NM_006005.3:c.792C>A