Canonical Allele Identifier: PA2825944046
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Ala735Val
CA015951
NM_001160161.2:c.2204C>T