Canonical Allele Identifier: PA307102
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ser88Gly
CA016327
NM_001099404.2:c.262A>G