Allele Registry

Canonical Allele Identifier: PA2825129438

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003655192

RCV003999582

ClinVar Variation:

571359

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.His557Tyr	CA058468 NM_000335.5:c.1669C>T