Allele Registry

Canonical Allele Identifier: PA265819

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058757

ClinVar Variation:

67971

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Lys175Asn	CA019045 NM_000335.5:c.525G>C CA352153868 NM_000335.5:c.525G>T