Canonical Allele Identifier: PA2825128171
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2985529
ClinVar RCV Id: RCV003841136
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Leu39Val
CA352158796
NM_000335.5:c.115T>G