Canonical Allele Identifier: PA174693
Gene: PDP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 161736
ClinVar RCV Id: RCV000149272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065837.1:p.Asn297Ser
CA174692
NM_020786.4:c.890A>G