Canonical Allele Identifier: PA307894
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Gln1909Arg
CA019443
NM_001099404.2:c.5726A>G