Canonical Allele Identifier: PA2825129606
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2995078
ClinVar RCV Id: RCV003850685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Pro627Ala
CA352145806
NM_000335.5:c.1879C>G