Canonical Allele Identifier: PA2825944057
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1505367
ClinVar RCV Id: RCV003657620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Asn740Lys
CA352144509
NM_001160161.2:c.2220C>G
CA352144510
NM_001160161.2:c.2220C>A