Canonical Allele Identifier: PA2825941267
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1063926
ClinVar RCV Id: RCV003771206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Phe934Ser
CA352140765
NM_001160160.2:c.2801T>C