Canonical Allele Identifier: PA2825490750
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2005605
ClinVar RCV Id: RCV003658202

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ile1673Asn
CA352142733
NM_001099404.2:c.5018T>A