Canonical Allele Identifier: PA2825496686
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg1626His
CA018760
NM_001099405.2:c.4877G>A