Canonical Allele Identifier: PA2827557156
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 5299
ClinVar RCV Id: RCV000005620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Gln271Arg
CA011596
NM_001350650.2:c.812A>G