Canonical Allele Identifier: PA2573289004
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1413521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Ser1833Ala
CA7534398
NM_025137.4:c.5497T>G