Canonical Allele Identifier: PA2825945126
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Met1444Val
CA018339
NM_001160161.2:c.4330A>G