Canonical Allele Identifier: PA2825944765
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67827
ClinVar RCV Id: RCV000058603

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Trp1217Cys
CA017524
NM_001160161.2:c.3651G>C
CA352148951
NM_001160161.2:c.3651G>T