Canonical Allele Identifier: PA2827921989
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201576

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Arg569Gly
CA015193
NM_001354701.2:c.1705C>G