Allele Registry

Canonical Allele Identifier: PA2827921971

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003655192

RCV003999582

ClinVar Variation:

571359

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341630.1:p.His557Tyr	CA058468 NM_001354701.2:c.1669C>T