Canonical Allele Identifier: PA2825490200
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 987837
ClinVar RCV Id: RCV001269191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Asn1472Ile
CA352145258
NM_001099404.2:c.4415A>T