Canonical Allele Identifier: PA2825431759
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 406843
ClinVar RCV Id: RCV000466459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041639.1:p.Leu373Met
CA16610110
NM_001048174.1:c.1117C>A