Canonical Allele Identifier: PA2825129060
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1017347
ClinVar RCV Id: RCV003541337
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Gly400Arg
CA352148872
NM_000335.5:c.1198G>C
CA352148874
NM_000335.5:c.1198G>A