Allele Registry

Canonical Allele Identifier: PA2573277780

Gene: MCCC2 HGNC NCBI

ClinVar RCV:

RCV001998721

ClinVar Variation:

1483322

HGVS (amino-acid)	Matching Registered Transcripts
NP_071415.1:p.Thr556Ile	CA120008692 NM_022132.5:c.1667C>T