Allele Registry

Canonical Allele Identifier: PA101951

Gene: NHP2 HGNC NCBI

ClinVar RCV:

RCV000004501

RCV000032277

ClinVar Variation:

4280

HGVS (amino-acid)	Matching Registered Transcripts
NP_060308.1:p.Tyr139His	CA016069 NM_017838.4:c.415T>C