Allele Registry

Canonical Allele Identifier: PA349348

Gene: SPG7 HGNC NCBI

ClinVar Allele:

222537

ClinVar RCV:

RCV000205153

ClinVar Variation:

219638

HGVS (amino-acid)	Matching Registered Transcripts
NP_003110.1:p.Ile219Thr	CA349347 NM_003119.4:c.656T>C