Canonical Allele Identifier: PA2825375627
Gene: NHP2 HGNC NCBI
ClinVar RCV:
RCV002190022
ClinVar Variation:
1554146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030005.1:p.Ala87Gly
CA362391163
NM_001034833.2:c.260C>G