Canonical Allele Identifier: PA2825489821
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2089349
ClinVar RCV Id: RCV003658495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Leu1371Val
CA352146918
NM_001099404.2:c.4111T>G