Allele Registry

Canonical Allele Identifier: PA103581

Gene: NOP10 HGNC NCBI

ClinVar RCV:

RCV000004500

ClinVar Variation:

4279

HGVS (amino-acid)	Matching Registered Transcripts
NP_061118.1:p.Arg34Trp	CA020161 NM_018648.4:c.100C>T