Canonical Allele Identifier: PA2825129538
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_000326.2:p.Asn598Asp
CA352146143
NM_000335.5:c.1792A>G