Allele Registry

Canonical Allele Identifier: PA307297

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003658492

ClinVar Variation:

2089206

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Ser528Arg	CA015016 NM_198056.3:c.1584C>A CA352147346 NM_198056.3:c.1584C>G CA352147368 NM_198056.3:c.1582A>C