Canonical Allele Identifier: PA2825426657
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041636.2:p.Arg281Cys
CA011853
NM_001048171.2:c.841C>T