Canonical Allele Identifier: PA2826828487
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 230638

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280124.1:p.Ser276Arg
CA059578
NM_001293195.2:c.828C>G
CA340134348
NM_001293195.2:c.828C>A
CA340134358
NM_001293195.2:c.826A>C