Canonical Allele Identifier: PA2827557120
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 406843
ClinVar RCV Id: RCV000466459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Leu258Met
CA16610110
NM_001350650.2:c.772C>A