Canonical Allele Identifier: PA1139683779
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 928029
ClinVar RCV Id: RCV001191678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Thr468Ala
CA340132645
NM_001128425.2:c.1402A>G