Canonical Allele Identifier: PA1139761727
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 959368
ClinVar RCV Id: RCV001232708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Leu2150Val
CA392216289
NM_025137.4:c.6448C>G