Canonical Allele Identifier: PA2825942831
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68013
ClinVar RCV Id: RCV000058809 RCV001545225
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Ala1916Ser
CA019500
NM_001160160.2:c.5746G>T