Canonical Allele Identifier: PA645389610
Gene: PNP HGNC NCBI

Linked Data

ClinVar Variation Id: 373674
ClinVar RCV Id: RCV000413493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000261.2:p.Gly90Arg
CA7082058
NM_000270.4:c.268G>A
CA389145022
NM_000270.4:c.268G>C