Allele Registry

Canonical Allele Identifier: PA096142

Gene: MMUT HGNC NCBI

ClinVar RCV:

RCV000478937

RCV000667041

ClinVar Variation:

418341

HGVS (amino-acid)	Matching Registered Transcripts
NP_000246.2:p.Gly215Cys	CA16618294 NM_000255.4:c.643G>T