Canonical Allele Identifier: PA2573165387
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 1487103
ClinVar RCV Id: RCV002033461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Val487Phe
CA364397286
NM_000255.4:c.1459G>T