Canonical Allele Identifier: PA2825940548
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1171478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Leu441Phe
CA057516
NM_001160160.2:c.1321C>T