Canonical Allele Identifier: PA2825537719
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3073752
ClinVar RCV Id: RCV004016758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ala296Thr
CA352150411
NM_001099404.2:c.886G>A