Canonical Allele Identifier: PA2825944893
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67855
ClinVar RCV Id: RCV000058634

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Ile1296Thr
CA017817
NM_001160161.2:c.3887T>C