Canonical Allele Identifier: PA2825940193
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201434
ClinVar RCV Id: RCV000619019

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.His184Gln
CA019320
NM_001160160.2:c.552C>G
CA352153775
NM_001160160.2:c.552C>A