Canonical Allele Identifier: PA2825942171
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Leu1500Val
CA018357
NM_001160160.2:c.4498C>G