Canonical Allele Identifier: PA645453588
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 374486
ClinVar RCV Id: RCV000415927 RCV003505109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Gln1301del
CA8709118
NM_000334.4:c.3901_3903del