Allele Registry

Canonical Allele Identifier: PA658670755

Gene: SPG7 HGNC NCBI

ClinVar RCV:

RCV000520300

RCV001066395

ClinVar Variation:

451927

HGVS (amino-acid)	Matching Registered Transcripts
NP_003110.1:p.Thr644Ile	CA397432955 NM_003119.4:c.1931C>T