Canonical Allele Identifier: PA2825429922
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 182695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041638.1:p.Ser296Leu
CA014753
NM_001048173.1:c.887C>T