Canonical Allele Identifier: PA2825945247
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Arg1529Cys
CA018516
NM_001160161.2:c.4585C>T