Canonical Allele Identifier: PA2827921471
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1722487
ClinVar RCV Id: RCV002302601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Phe198Leu
CA352153494
NM_001354701.2:c.594T>G
CA352153495
NM_001354701.2:c.594T>A
CA352153510
NM_001354701.2:c.592T>C