Canonical Allele Identifier: PA2825941823
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67831

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Leu1282Met
CA017562
NM_001160160.2:c.3844C>A