Canonical Allele Identifier: PA658665388
Gene: MCCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071415.1:p.Arg332Gln
CA3297946
NM_022132.5:c.995G>A