Canonical Allele Identifier: PA2573165362
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 1422287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Thr387Pro
CA364398995
NM_000255.4:c.1159A>C