Canonical Allele Identifier: PA645435159
Gene: MMUT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Glu276Asp
CA10575876
NM_000255.4:c.828G>C
CA364402297
NM_000255.4:c.828G>T