Canonical Allele Identifier: PA658668916
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 477418
ClinVar RCV Id: RCV000534297 RCV000658059
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Glu1208Gln
CA8709222
NM_000334.4:c.3622G>C