Allele Registry

Canonical Allele Identifier: PA2828080188

Gene: MCCC2 HGNC NCBI

ClinVar RCV:

RCV001998721

ClinVar Variation:

1483322

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350076.1:p.Thr518Ile	CA120008692 NM_001363147.1:c.1553C>T