Canonical Allele Identifier: PA2828080032
Gene: MCCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350076.1:p.Arg294Gln
CA3297946
NM_001363147.1:c.881G>A