Canonical Allele Identifier: PA101913
Gene: PNP HGNC NCBI

Linked Data

ClinVar Variation Id: 13990
ClinVar RCV Id: RCV000015027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000261.2:p.Asp128Gly
CA123673
NM_000270.4:c.383A>G