Canonical Allele Identifier: PA2827924014
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 219835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Val1884Leu
CA348136
NM_001354701.2:c.5650G>T
CA352140249
NM_001354701.2:c.5650G>C