Canonical Allele Identifier: PA101922
Gene: PNP HGNC NCBI
ClinVar RCV:
RCV000015025
ClinVar Variation:
13988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000261.2:p.Glu89Lys
CA123669
NM_000270.4:c.265G>A