Canonical Allele Identifier: PA218880
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67766

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg971Cys
CA016616
NM_001099404.2:c.2911C>T