Canonical Allele Identifier: PA1139683660
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 992066

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Val500Ala
CA138795784
NM_000255.4:c.1499T>C