Canonical Allele Identifier: PA2825495030
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Glu1053Lys
CA016871
NM_001099405.2:c.3157G>A