Canonical Allele Identifier: PA096197
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 218990
ClinVar RCV Id: RCV000203344 RCV000723412 RCV000588430 RCV001271706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Gly427Asp
CA347873
NM_000255.4:c.1280G>A