Allele Registry

Canonical Allele Identifier: PA110221

Gene: MCCC2 HGNC NCBI

ClinVar RCV:

RCV000179523

RCV000185999

RCV002298507

ClinVar Variation:

198252

HGVS (amino-acid)	Matching Registered Transcripts
NP_071415.1:p.His190Tyr	CA275357 NM_022132.5:c.568C>T