Allele Registry

Canonical Allele Identifier: PA2825945590

Gene: SCN5A HGNC NCBI

ClinVar Allele:

78881

ClinVar RCV:

RCV000058776

RCV003542282

ClinVar Variation:

67989

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153633.1:p.Asp1736Gly	CA019174 NM_001160161.2:c.5207A>G