Canonical Allele Identifier: PA2825943499
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Thr370Met
CA014345
NM_001160161.2:c.1109C>T