Canonical Allele Identifier: PA2825132558
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 519340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ile1852Val
CA352140852
NM_000335.5:c.5554A>G