Canonical Allele Identifier: PA1139680957
Gene: PNP HGNC NCBI

Linked Data

ClinVar Variation Id: 861659
ClinVar RCV Id: RCV001068226
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000261.2:p.Val61Leu
CA389144820
NM_000270.4:c.181G>C
CA389144821
NM_000270.4:c.181G>T