Canonical Allele Identifier: PA2825943259
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 222801
ClinVar RCV Id: RCV000208056 RCV000457388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Thr187Ala
CA351742
NM_001160161.2:c.559A>G