Canonical Allele Identifier: PA1139683237
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 909695
ClinVar RCV Id: RCV001160921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Ala191Val
CA364404436
NM_000255.4:c.572C>T