Canonical Allele Identifier: PA2825941935
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Val1352Met
CA017837
NM_001160160.2:c.4054G>A