Canonical Allele Identifier: PA096601
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 1878
ClinVar RCV Id: RCV000001955 RCV000203407 RCV000374459 RCV001271724 RCV003114172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Trp105Arg
CA249727
NM_000255.4:c.313T>C
CA364405021
NM_000255.4:c.313T>A