Canonical Allele Identifier: PA1139683828
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 946121
ClinVar RCV Id: RCV001216914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Glu480Val
CA340132584
NM_001128425.2:c.1439A>T