Allele Registry

Canonical Allele Identifier: PA108621

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000009999

RCV000058777

ClinVar Variation:

9397

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Tyr1795His	CA019191 NM_198056.3:c.5383T>C