Canonical Allele Identifier: PA2573287791
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1349540
ClinVar RCV Id: RCV002046996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Ser92Phe
CA270111031
NM_025137.4:c.275C>T