Canonical Allele Identifier: PA2825128304
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1384596
ClinVar RCV Id: RCV003657396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Asp84Gly
CA352157870
NM_000335.5:c.251A>G