Canonical Allele Identifier: PA307615
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67849

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val1339Ile
CA017761
NM_000335.5:c.4015G>A