Canonical Allele Identifier: PA2825945811
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 999632
ClinVar RCV Id: RCV003656785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Phe1874Val
CA352139966
NM_001160161.2:c.5620T>G