Canonical Allele Identifier: PA2825941133
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67739
ClinVar RCV Id: RCV000058508 RCV000183178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Thr843Ala
CA016243
NM_001160160.2:c.2527A>G