Allele Registry

Canonical Allele Identifier: PA916062760

Gene: SPG7 HGNC NCBI

ClinVar RCV:

RCV000205153

ClinVar Variation:

219638

HGVS (amino-acid)	Matching Registered Transcripts
NP_955399.1:p.Ile219Thr	CA349347 NM_199367.3:c.656T>C