Canonical Allele Identifier: PA329985
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg1174Cys
CA017218
NM_000335.5:c.3520C>T