Canonical Allele Identifier: PA2825945776
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Gln1855Arg
CA019443
NM_001160161.2:c.5564A>G