Canonical Allele Identifier: PA2825941840
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2500084
ClinVar RCV Id: RCV003224731
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Ala1293Thr
CA352148215
NM_001160160.2:c.3877G>A