Canonical Allele Identifier: PA2826823129
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280119.1:p.Ser24Gly
CA011818
NM_001293190.2:c.70A>G