Allele Registry

Canonical Allele Identifier: PA201912

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058614

RCV000148841

RCV000176338

RCV000243761

RCV000987205

RCV001842355

ClinVar Variation:

67836

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Leu1308Phe	CA017626 NM_001099404.2:c.3922C>T CA085417 NM_001099404.2:c.[3922C>T;703+223G>A]