Canonical Allele Identifier: PA2580266125
Gene: PTPRD HGNC NCBI
ClinVar RCV:
RCV004077618
ClinVar Variation:
2212918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002830.1:p.Gln1010Arg
CA4983937
NM_002839.4:c.3029A>G