Allele Registry

Canonical Allele Identifier: PA1139683237

Gene: MMUT HGNC NCBI

ClinVar RCV:

RCV001160921

ClinVar Variation:

909695

HGVS (amino-acid)	Matching Registered Transcripts
NP_000246.2:p.Ala191Val	CA364404436 NM_000255.4:c.572C>T