Canonical Allele Identifier: PA2825945483
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Asp1675Asn
CA018973
NM_001160161.2:c.5023G>A