Canonical Allele Identifier: PA2825497432
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Gln1891Arg
CA019443
NM_001099405.2:c.5672A>G