Canonical Allele Identifier: PA2827921254
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1388876
ClinVar RCV Id: RCV003772680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Gln55Leu
CA352158425
NM_001354701.2:c.164A>T