Canonical Allele Identifier: PA2828732942
Gene: PTPRD HGNC NCBI
ClinVar RCV:
RCV004077618
ClinVar Variation:
2212918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364887.1:p.Gln1010Arg
CA4983937
NM_001377958.1:c.3029A>G