Canonical Allele Identifier: PA645408119
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 284018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Ala106Thr
CA7535871
NM_025137.4:c.316G>A