Allele Registry

Canonical Allele Identifier: PA096580

Gene: MMUT HGNC NCBI

ClinVar RCV:

RCV000186047

ClinVar Variation:

203847

HGVS (amino-acid)	Matching Registered Transcripts
NP_000246.2:p.Thr370Pro	CA312765 NM_000255.4:c.1108A>C