Canonical Allele Identifier: PA2499230129
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 1071892
ClinVar RCV Id: RCV001384464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Val136Phe
CA364404792
NM_000255.4:c.406G>T