Canonical Allele Identifier: PA2825432141
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 483938

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041639.1:p.Ser490Arg
CA340131824
NM_001048174.1:c.1470T>G
CA340131828
NM_001048174.1:c.1470T>A
CA340131837
NM_001048174.1:c.1468A>C