Canonical Allele Identifier: PA645453298
Gene: NHP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 241215
ClinVar RCV Id: RCV000231896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060308.1:p.Met128Thr
CA3589116
NM_017838.4:c.383T>C