Canonical Allele Identifier: PA658804209
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 523066

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Pro64Leu
CA3847168
NM_000255.4:c.191C>T