Allele Registry

Canonical Allele Identifier: PA2580450195

Gene: MCCC2 HGNC NCBI

ClinVar Allele:

1917774

ClinVar RCV:

RCV002606637

ClinVar Variation:

2186430

HGVS (amino-acid)	Matching Registered Transcripts
NP_071415.1:p.Thr385Ala	CA3298056 NM_022132.5:c.1153A>G