Allele Registry

Canonical Allele Identifier: PA2828079895

Gene: MCCC2 HGNC NCBI

ClinVar RCV:

RCV001782421

ClinVar Variation:

1324701

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350076.1:p.Ser101Phe	CA3297739 NM_001363147.1:c.302C>T