Canonical Allele Identifier: PA196318
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 186948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Asp530His
CA013114
NM_001128425.2:c.1588G>C