Canonical Allele Identifier: PA916018670
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280124.1:p.Val8Met
CA011797
NM_001293195.2:c.22G>A