Canonical Allele Identifier: PA2825491389
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 449118
ClinVar RCV Id: RCV000520769 RCV001841409 RCV002350145
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Pro1884Leu
CA064584
NM_001099404.2:c.5651C>T