Canonical Allele Identifier: PA322016
Gene: SPG7 HGNC NCBI

Linked Data

ClinVar Variation Id: 215223
ClinVar RCV Id: RCV000197553 RCV001233181 RCV001847891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003110.1:p.Ser576Trp
CA322015
NM_003119.4:c.1727C>G