Canonical Allele Identifier: PA645389593
Gene: PNP HGNC NCBI

Linked Data

ClinVar Variation Id: 312728
ClinVar RCV Id: RCV000391224
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000261.2:p.Lys22Asn
CA10639848
NM_000270.4:c.66G>C
CA389144280
NM_000270.4:c.66G>T