Canonical Allele Identifier: PA2499291609
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1046780
ClinVar RCV Id: RCV001351383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Tyr1238Cys
CA270092836
NM_025137.4:c.3713A>G