Canonical Allele Identifier: PA2825497298
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 519340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Ile1835Val
CA352140852
NM_001099405.2:c.5503A>G