Canonical Allele Identifier: PA2825427192
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 490032
ClinVar RCV Id: RCV000580166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041636.2:p.Thr455Ile
CA340132546
NM_001048171.2:c.1364C>T