Allele Registry

Canonical Allele Identifier: PA2828080067

Gene: MCCC2 HGNC NCBI

ClinVar RCV:

RCV003417026

RCV003498001

ClinVar Variation:

2634083

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350076.1:p.Phe349Val	CA359994140 NM_001363147.1:c.1045T>G