Canonical Allele Identifier: PA2826827153
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 421574
ClinVar RCV Id: RCV000481734

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Gly276Ser
CA16617156
NM_001293192.2:c.826G>A