Canonical Allele Identifier: PA2825491419
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 406444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg1897Gln
CA064637
NM_001099404.2:c.5690G>A