Allele Registry

Canonical Allele Identifier: PA110349

Gene: MCCC2 HGNC NCBI

ClinVar RCV:

RCV001378263

ClinVar Variation:

203803

HGVS (amino-acid)	Matching Registered Transcripts
NP_071415.1:p.Ser173Leu	CA312686 NM_022132.5:c.518C>T