Canonical Allele Identifier: PA2825079113
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 3178992
ClinVar RCV Id: RCV004475364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Ser22Leu
CA3847182
NM_000255.4:c.65C>T