Canonical Allele Identifier: PA287864
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 127837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Thr434Met
CA012538
NM_001128425.2:c.1301C>T