Canonical Allele Identifier: PA2825496105
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 418616
ClinVar RCV Id: RCV000481094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Tyr1429His
CA16617946
NM_001099405.2:c.4285T>C