Canonical Allele Identifier: PA2826827393
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 219673
ClinVar RCV Id: RCV000206030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Pro351Thr
CA350097
NM_001293192.2:c.1051C>A