Canonical Allele Identifier: PA645434936
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 374213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Pro95Leu
CA3847144
NM_000255.4:c.284C>T