Canonical Allele Identifier: PA2826825687
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 926218
ClinVar Variation Id: 2111333
ClinVar RCV Id: RCV003023932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280120.1:p.Asp333Glu
CA060205
NM_001293191.2:c.999C>A
CA340133753
NM_001293191.2:c.999C>G