Canonical Allele Identifier: PA2825495836
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67840
ClinVar RCV Id: RCV000058619 RCV000183188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Ala1326Ser
CA017686
NM_001099405.2:c.3976G>T