Canonical Allele Identifier: PA2827924023
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Gln1890Arg
CA019443
NM_001354701.2:c.5669A>G