Canonical Allele Identifier: PA2825129971
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 629558
ClinVar RCV Id: RCV001841936
ClinVar Variation Id: 929106
ClinVar RCV Id: RCV001194084

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Met801Ile
CA352143245
NM_000335.5:c.2403G>T
CA352143246
NM_000335.5:c.2403G>C
CA352143247
NM_000335.5:c.2403G>A