Canonical Allele Identifier: PA2825941298
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Asp953Glu
CA016578
NM_001160160.2:c.2859C>G
CA352140500
NM_001160160.2:c.2859C>A