Canonical Allele Identifier: PA2827556941
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41767
ClinVar Variation Id: 492713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Gln195His
CA011883
NM_001350650.2:c.585G>C
CA340133885
NM_001350650.2:c.585G>T