Canonical Allele Identifier: PA117216
Gene: MINPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 5022
ClinVar RCV Id: RCV000005325
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Amino-acid Alleles

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