Canonical Allele Identifier: PA2580109689
Gene: PNP HGNC NCBI

Linked Data

ClinVar Variation Id: 1926676
ClinVar RCV Id: RCV002605302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000261.2:p.Ile29Met
CA389144378
NM_000270.4:c.87A>G