Canonical Allele Identifier: PA2573165386
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 1416035
ClinVar RCV Id: RCV001933380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Ser483Pro
CA3846873
NM_000255.4:c.1447T>C