Canonical Allele Identifier: PA2825942329
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1188516
ClinVar RCV Id: RCV001548332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Arg1605Leu
CA352142977
NM_001160160.2:c.4814G>T