Canonical Allele Identifier: PA658809268
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 532098
ClinVar RCV Id: RCV003539997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Arg282Gly
CA352150552
NM_198056.3:c.844C>G