Canonical Allele Identifier: PA2825940395
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Arg340Trp
CA014168
NM_001160160.2:c.1018C>T