Canonical Allele Identifier: PA2826827172
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 662771
ClinVar RCV Id: RCV000820500
ClinVar Variation Id: 818576

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Glu283Asp
CA340133116
NM_001293192.2:c.849G>T
CA340133119
NM_001293192.2:c.849G>C