Canonical Allele Identifier: PA2826824036
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 185982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280119.1:p.Ser333Trp
CA012006
NM_001293190.2:c.998C>G