Allele Registry

Canonical Allele Identifier: PA142968

Gene: SCN5A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000041594

RCV000058380

RCV000244721

RCV000263131

RCV000277696

RCV000318270

RCV000357684

RCV000372880

RCV001094908

RCV001841583

ClinVar Variation:

48279

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Arg34Cys	CA014158 NM_198056.3:c.100C>T