Canonical Allele Identifier: PA2825131455
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 519279
ClinVar RCV Id: RCV000619930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala1426Glu
CA352145580
NM_000335.5:c.4277C>A