Canonical Allele Identifier: PA658804742
Gene: PNP HGNC NCBI

Linked Data

ClinVar Variation Id: 501882
ClinVar RCV Id: RCV000592494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000261.2:p.His20Gln
CA389144246
NM_000270.4:c.60C>G
CA389144248
NM_000270.4:c.60C>A