Canonical Allele Identifier: PA2825942761
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Gln1876Arg
CA019443
NM_001160160.2:c.5627A>G