Canonical Allele Identifier: PA2825945916
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 30045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Asn1933Lys
CA019555
NM_001160161.2:c.5799C>A
CA352139301
NM_001160161.2:c.5799C>G