Canonical Allele Identifier: PA101961
Gene: NHP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4281
ClinVar RCV Id: RCV000004502 RCV000032276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060308.1:p.Val126Met
CA016060
NM_017838.4:c.376G>A