Canonical Allele Identifier: PA2825079638
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 3178117
ClinVar RCV Id: RCV004472506

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Met431Thr
CA138796325
NM_000255.4:c.1292T>C