Canonical Allele Identifier: PA2826827598
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Arg414Gln
CA011691
NM_001293192.2:c.1241G>A