Canonical Allele Identifier: PA2827557569
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 492027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Asp397Asn
CA340131573
NM_001350650.2:c.1189G>A