Canonical Allele Identifier: PA2825941888
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Asn1324Ser
CA017679
NM_001160160.2:c.3971A>G