Allele Registry

Canonical Allele Identifier: PA211816

Gene: SCN5A HGNC NCBI

Linked Data

ClinVar RCV:

RCV000058771

RCV000148849

RCV000183115

RCV000617171

RCV000786219

RCV001146112

RCV001146113

RCV001146114

RCV001146115

RCV001146116

RCV001146117

RCV001842384

ClinVar Variation:

67985

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Thr1779Met	CA019134 NM_001099404.2:c.5336C>T