Canonical Allele Identifier: PA2825941902
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Pro1331Leu
CA017721
NM_001160160.2:c.3992C>T