Allele Registry

Canonical Allele Identifier: PA658665409

Gene: MCCC2 HGNC NCBI

ClinVar RCV:

RCV000532761

ClinVar Variation:

467804

HGVS (amino-acid)	Matching Registered Transcripts
NP_071415.1:p.Thr484Pro	CA359999203 NM_022132.5:c.1450A>C