Canonical Allele Identifier: PA2825537389
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1035042
ClinVar RCV Id: RCV003541353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ser11Arg
CA72951853
NM_001099404.2:c.33C>A
CA352159498
NM_001099404.2:c.33C>G
CA352159521
NM_001099404.2:c.31A>C