Allele Registry

Canonical Allele Identifier: PA2573277627

Gene: MCCC2 HGNC NCBI

ClinVar Allele:

1480030

ClinVar RCV:

RCV001927701

ClinVar Variation:

1404333

HGVS (amino-acid)	Matching Registered Transcripts
NP_071415.1:p.Thr385Ser	CA359994058 NM_022132.5:c.1153A>T CA359994065 NM_022132.5:c.1154C>G