Canonical Allele Identifier: PA645434929
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 235300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Ile69Val
CA3847163
NM_000255.4:c.205A>G