Canonical Allele Identifier: PA2741812022
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 2919978
ClinVar RCV Id: RCV003736102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Gly427Ser
CA364398741
NM_000255.4:c.1279G>A