Canonical Allele Identifier: PA2825941759
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1354300
ClinVar RCV Id: RCV003772461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Val1236Ala
CA352149337
NM_001160160.2:c.3707T>C