Allele Registry

Canonical Allele Identifier: PA2825942467

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058750

RCV003542279

ClinVar Variation:

67964

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153632.1:p.Cys1695Trp	CA018961 NM_001160160.2:c.5085C>G