Canonical Allele Identifier: PA191588
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 185309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Ala205Thr
CA013987
NM_001128425.2:c.613G>A