Canonical Allele Identifier: PA330032
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67843
ClinVar RCV Id: RCV000058622 RCV003556153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ala1330Pro
CA017704
NM_001099404.2:c.3988G>C