Canonical Allele Identifier: PA2827922030
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2774477
ClinVar RCV Id: RCV003592359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Asn598Asp
CA352146143
NM_001354701.2:c.1792A>G