Canonical Allele Identifier: PA095909
Gene: MMUT HGNC NCBI
ClinVar RCV:
RCV002013072
ClinVar Variation:
1499832
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Arg108Gly
CA364404999
NM_000255.4:c.322C>G