Allele Registry

Canonical Allele Identifier: PA265856

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058792

RCV001842388

RCV002477204

RCV003541030

ClinVar Variation:

67998

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Ala185Val	CA019348 NM_198056.3:c.554C>T