Allele Registry

Canonical Allele Identifier: PA117216

Gene: MINPP1 HGNC NCBI

ClinVar Allele:

20061

ClinVar RCV:

RCV000005325

ClinVar Variation:

5022

HGVS (amino-acid)	Matching Registered Transcripts
NP_004888.2:p.Gln270Arg	CA117215 NM_004897.5:c.809A>G