Canonical Allele Identifier: PA2826823109
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280119.1:p.Pro18Leu
CA011771
NM_001293190.2:c.53C>T