Canonical Allele Identifier: PA2825944889
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1737287
ClinVar RCV Id: RCV002321206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Ile1293Thr
CA352147360
NM_001160161.2:c.3878T>C