Canonical Allele Identifier: PA2825943875
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 978332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.His617Leu
CA72939070
NM_001160161.2:c.1850A>T