Canonical Allele Identifier: PA1139683169
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 934764
ClinVar RCV Id: RCV002561121

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Met99Thr
CA364405059
NM_000255.4:c.296T>C