Allele Registry

Canonical Allele Identifier: PA2828080066

Gene: MCCC2 HGNC NCBI

ClinVar Allele:

1480030

ClinVar RCV:

RCV001927701

ClinVar Variation:

1404333

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350076.1:p.Thr347Ser	CA359994058 NM_001363147.1:c.1039A>T CA359994065 NM_001363147.1:c.1040C>G