Canonical Allele Identifier: PA143106
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 48306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg18Gln
CA019208
NM_001099404.2:c.53G>A