Allele Registry

Canonical Allele Identifier: PA096529

Gene: MMUT HGNC NCBI

ClinVar RCV:

RCV000203360

ClinVar Variation:

218985

HGVS (amino-acid)	Matching Registered Transcripts
NP_000246.2:p.Pro95Arg	CA347886 NM_000255.4:c.284C>G