Canonical Allele Identifier: PA2826076500
Gene: PTPRD HGNC NCBI
ClinVar RCV:
RCV001281520
ClinVar Variation:
992772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164496.1:p.Glu953Lys
CA188818863
NM_001171025.2:c.2857G>A