Allele Registry

Canonical Allele Identifier: PA2825945599

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000009999

RCV000058777

ClinVar Variation:

9397

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153633.1:p.Tyr1741His	CA019191 NM_001160161.2:c.5221T>C