Canonical Allele Identifier: PA2825941927
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1737287
ClinVar RCV Id: RCV002321206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Ile1346Thr
CA352147360
NM_001160160.2:c.4037T>C