Allele Registry

Canonical Allele Identifier: PA1139758707

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003541300

ClinVar Variation:

953630

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Ala572Gly	CA72939170 NM_198056.3:c.1715C>G