Canonical Allele Identifier: PA2499231319
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1191480
ClinVar RCV Id: RCV001552574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.His1726Arg
CA400613597
NM_000334.4:c.5177A>G