Canonical Allele Identifier: PA2825496663
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1189625
ClinVar RCV Id: RCV001550047
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Gly1621Glu
CA352142972
NM_001099405.2:c.4862G>A