Canonical Allele Identifier: PA2827556921
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1002430

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Ala190Val
CA340133943
NM_001350650.2:c.569C>T