Canonical Allele Identifier: PA330123
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67922
ClinVar RCV Id: RCV000058703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ile1592Met
CA018537
NM_000335.5:c.4776C>G