Canonical Allele Identifier: PA143050
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 48295

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val924Ile
CA016475
NM_000335.5:c.2770G>A