Canonical Allele Identifier: PA915955281
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 638964
ClinVar RCV Id: RCV001297506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Gln132Leu
CA364404815
NM_000255.4:c.395A>T