Allele Registry

Canonical Allele Identifier: PA2828080129

Gene: MCCC2 HGNC NCBI

ClinVar RCV:

RCV000532761

ClinVar Variation:

467804

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350076.1:p.Thr446Pro	CA359999203 NM_001363147.1:c.1336A>C