Canonical Allele Identifier: PA2825942279
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1743446
ClinVar RCV Id: RCV002330776

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Ile1578Thr
CA352143135
NM_001160160.2:c.4733T>C