Allele Registry

Canonical Allele Identifier: PA312772

Gene: MMUT HGNC NCBI

ClinVar RCV:

RCV000186051

ClinVar Variation:

203851

HGVS (amino-acid)	Matching Registered Transcripts
NP_000246.2:p.Arg629Gly	CA312771 NM_000255.4:c.1885A>G