Canonical Allele Identifier: PA307864
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201539
ClinVar RCV Id: RCV000183124 RCV000477269 RCV001842927 RCV002345636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ala1828Thr
CA019290
NM_001099404.2:c.5482G>A