Canonical Allele Identifier: PA2825491613
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3069459
ClinVar RCV Id: RCV004008003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ser1966Pro
CA352139533
NM_001099404.2:c.5896T>C