Canonical Allele Identifier: PA658800633
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 543797
ClinVar RCV Id: RCV000654648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Gln1300Glu
CA400617242
NM_000334.4:c.3898C>G