Canonical Allele Identifier: PA2826825611
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 182695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280120.1:p.Ser307Leu
CA014753
NM_001293191.2:c.920C>T