Canonical Allele Identifier: PA307893
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Gln1908Arg
CA019443
NM_000335.5:c.5723A>G