Canonical Allele Identifier: PA2825494364
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 629558
ClinVar RCV Id: RCV001841936
ClinVar Variation Id: 929106
ClinVar RCV Id: RCV001194084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Met801Ile
CA352143245
NM_001099405.2:c.2403G>T
CA352143246
NM_001099405.2:c.2403G>C
CA352143247
NM_001099405.2:c.2403G>A