Canonical Allele Identifier: PA2825429913
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 230146
ClinVar Variation Id: 439221

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041638.1:p.Gly293Arg
CA059784
NM_001048173.1:c.877G>A
CA340134139
NM_001048173.1:c.877G>C