Canonical Allele Identifier: PA2827557387
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 490032
ClinVar RCV Id: RCV000580166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Thr340Ile
CA340132546
NM_001350650.2:c.1019C>T