Canonical Allele Identifier: PA2825492337
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201434
ClinVar RCV Id: RCV000619019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.His184Gln
CA019320
NM_001099405.2:c.552C>G
CA352153775
NM_001099405.2:c.552C>A