Canonical Allele Identifier: PA2825130253
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3070886
ClinVar RCV Id: RCV004014388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala936Gly
CA352140741
NM_000335.5:c.2807C>G