Canonical Allele Identifier: PA2828737034
Gene: PTPRD HGNC NCBI
ClinVar RCV:
RCV001281520
ClinVar Variation:
992772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364987.1:p.Glu1365Lys
CA188818863
NM_001378058.1:c.4093G>A