Canonical Allele Identifier: PA2825940096
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2774498
ClinVar RCV Id: RCV003592380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.His118Pro
CA352156956
NM_001160160.2:c.353A>C