Allele Registry

Canonical Allele Identifier: PA312770

Gene: MMUT HGNC NCBI

ClinVar RCV:

RCV000186050

RCV000210837

ClinVar Variation:

203850

HGVS (amino-acid)	Matching Registered Transcripts
NP_000246.2:p.Ala555Thr	CA312769 NM_000255.4:c.1663G>A