Canonical Allele Identifier: PA916018683
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 141994
ClinVar Variation Id: 639290

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280125.1:p.Gly31Arg
CA013601
NM_001293196.2:c.91G>A
CA340136087
NM_001293196.2:c.91G>C