Canonical Allele Identifier: PA2827557439
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 216871

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Gln357_Gln358delinsCysTrp
CA338806
NM_001350650.2:c.1069_1073delinsTGTTG