Allele Registry

Canonical Allele Identifier: PA110150

Gene: MCCC2 HGNC NCBI

ClinVar RCV:

RCV000001997

RCV000082095

ClinVar Variation:

1920

HGVS (amino-acid)	Matching Registered Transcripts
NP_071415.1:p.Glu99Gln	CA223633 NM_022132.5:c.295G>C