Allele Registry

Canonical Allele Identifier: PA312785

Gene: MMUT HGNC NCBI

ClinVar RCV:

RCV000210836

RCV001271801

RCV001391331

ClinVar Variation:

203859

HGVS (amino-acid)	Matching Registered Transcripts
NP_000246.2:p.Thr297Ile	CA312784 NM_000255.4:c.890C>T