Canonical Allele Identifier: PA2825429049
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041638.1:p.Ser10Gly
CA011818
NM_001048173.1:c.28A>G