Allele Registry

Canonical Allele Identifier: PA101961

Gene: NHP2 HGNC NCBI

ClinVar Allele:

19320

ClinVar RCV:

RCV000004502

RCV000032276

ClinVar Variation:

4281

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