Allele Registry

Canonical Allele Identifier: PA108598

Gene: SPG7 HGNC NCBI

ClinVar Allele:

21854

ClinVar RCV:

RCV000007217

ClinVar Variation:

6815

HGVS (amino-acid)	Matching Registered Transcripts
NP_003110.1:p.Ser692Thr	CA253965 NM_003119.4:c.2075G>C