Allele Registry

Canonical Allele Identifier: PA110109

Gene: MCCC2 HGNC NCBI

ClinVar RCV:

RCV000002004

ClinVar Variation:

1927

HGVS (amino-acid)	Matching Registered Transcripts
NP_071415.1:p.Asp280Tyr	CA251973 NM_022132.5:c.838G>T