Canonical Allele Identifier: PA2825495834
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Asn1325Ser
CA017679
NM_001099405.2:c.3974A>G