Canonical Allele Identifier: PA2825945840
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2797141
ClinVar RCV Id: RCV003671042

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Glu1891Asp
CA352139771
NM_001160161.2:c.5673G>T
CA352139772
NM_001160161.2:c.5673G>C