Canonical Allele Identifier: PA2829726468
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41767
ClinVar Variation Id: 492713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036354.1:p.Gln335His
CA011883
NM_012222.3:c.1005G>C
CA340133885
NM_012222.3:c.1005G>T