Allele Registry

Canonical Allele Identifier: PA2580450096

Gene: MCCC2 HGNC NCBI

ClinVar RCV:

RCV002286462

ClinVar Variation:

1707502

HGVS (amino-acid)	Matching Registered Transcripts
NP_071415.1:p.Arg59Gln	CA3297681 NM_022132.5:c.176G>A