Canonical Allele Identifier: PA2827557541
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 182685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Asp387Tyr
CA013123
NM_001350650.2:c.1159G>T