Canonical Allele Identifier: PA096137
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 218987
ClinVar RCV Id: RCV000203339 RCV001091103 RCV003317150 RCV001833168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Gly203Arg
CA347872
NM_000255.4:c.607G>A
CA364404367
NM_000255.4:c.607G>C