Canonical Allele Identifier: PA2825538819
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1172206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Glu1203Ala
CA352138102
NM_001099404.2:c.3608A>C