Canonical Allele Identifier: PA2580109962
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 1997706
ClinVar RCV Id: RCV002791911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Gly427Val
CA364398737
NM_000255.4:c.1280G>T
CA2580074725
NM_000255.4:c.1280_1281delinsTA