Allele Registry

Canonical Allele Identifier: PA2825939947

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV001842080

ClinVar Variation:

1171341

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153632.1:p.Arg27Leu	CA056875 NM_001160160.2:c.80G>T