Allele Registry

Canonical Allele Identifier: PA658814805

Gene: SPG11 HGNC NCBI

ClinVar RCV:

RCV000642530

RCV001507872

RCV002360574

RCV002467948

RCV002467949

ClinVar Variation:

534836

HGVS (amino-acid)	Matching Registered Transcripts
NP_079413.3:p.Asn2315Thr	CA7533946 NM_025137.4:c.6944A>C