Canonical Allele Identifier: PA101906
Gene: PNP HGNC NCBI

Linked Data

ClinVar Variation Id: 13991
ClinVar RCV Id: RCV000015028 RCV000419921 RCV002298444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000261.2:p.Arg234Pro
CA123675
NM_000270.4:c.701G>C