Canonical Allele Identifier: PA2826826942
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 182695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Ser204Leu
CA014753
NM_001293192.2:c.611C>T