Allele Registry

Canonical Allele Identifier: PA645430078

Gene: PTPRT HGNC NCBI

ClinVar RCV:

RCV000454261

ClinVar Variation:

402165

HGVS (amino-acid)	Matching Registered Transcripts
NP_573400.3:p.Val69Ala	CA9864900 NM_133170.4:c.206T>C