Canonical Allele Identifier: PA2573165360
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 1402699
ClinVar RCV Id: RCV001906557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Thr382Ala
CA364399028
NM_000255.4:c.1144A>G