Canonical Allele Identifier: PA2825128229
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1388876
ClinVar RCV Id: RCV003772680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Gln55Leu
CA352158425
NM_000335.5:c.164A>T