Canonical Allele Identifier: PA2827924152
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 520462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Val1961Phe
CA065024
NM_001354701.2:c.5881G>T