Canonical Allele Identifier: PA2827557383
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1772772
ClinVar RCV Id: RCV002394428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.His339Tyr
CA340132562
NM_001350650.2:c.1015C>T