Allele Registry

Canonical Allele Identifier: PA658665380

Gene: MCCC2 HGNC NCBI

ClinVar RCV:

RCV000556717

ClinVar Variation:

467808

HGVS (amino-acid)	Matching Registered Transcripts
NP_071415.1:p.Gly237Arg	CA359983581 NM_022132.5:c.709G>C