Canonical Allele Identifier: PA2826828502
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280124.1:p.Arg281Cys
CA011853
NM_001293195.2:c.841C>T