Canonical Allele Identifier: PA2825537428
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1524249
ClinVar RCV Id: RCV003657669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Thr38Ala
CA352158816
NM_001099404.2:c.112A>G