Canonical Allele Identifier: PA2580467735
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1915574
ClinVar RCV Id: RCV002601586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Thr1777Ser
CA392222781
NM_025137.4:c.5330C>G
CA392222783
NM_025137.4:c.5329A>T