Canonical Allele Identifier: PA215839
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Arg309Cys
CA011853
NM_001128425.2:c.925C>T