Canonical Allele Identifier: PA165065
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 141306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Glu196Asp
CA013929
NM_001128425.2:c.588G>C
CA340135446
NM_001128425.2:c.588G>T