Allele Registry

Canonical Allele Identifier: PA110180

Gene: MCCC2 HGNC NCBI

ClinVar RCV:

RCV002027785

RCV003403657

ClinVar Variation:

1521043

HGVS (amino-acid)	Matching Registered Transcripts
NP_071415.1:p.Gly352Arg	CA3297989 NM_022132.5:c.1054G>A CA359991460 NM_022132.5:c.1054G>C