Canonical Allele Identifier: PA2825944310
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 48295

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Val924Ile
CA016475
NM_001160161.2:c.2770G>A