Canonical Allele Identifier: PA2828736986
Gene: PTPRD HGNC NCBI
ClinVar RCV:
RCV004261812
ClinVar Variation:
2471300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364987.1:p.Gly902Cys
CA4984027
NM_001378058.1:c.2704G>T