Canonical Allele Identifier: PA2826829437
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 464736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280125.1:p.Thr112Ser
CA058731
NM_001293196.2:c.334A>T
CA340135237
NM_001293196.2:c.335C>G