Canonical Allele Identifier: PA2826828887
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 140816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280124.1:p.His407Tyr
CA012561
NM_001293195.2:c.1219C>T