Allele Registry

Canonical Allele Identifier: PA645435159

Gene: MMUT HGNC NCBI

ClinVar RCV:

RCV000236687

ClinVar Variation:

222921

HGVS (amino-acid)	Matching Registered Transcripts
NP_000246.2:p.Glu276Asp	CA10575876 NM_000255.4:c.828G>C CA364402297 NM_000255.4:c.828G>T