Canonical Allele Identifier: PA2829726819
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1770733
ClinVar RCV Id: RCV002383390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036354.1:p.Tyr450Ser
CA340132739
NM_012222.3:c.1349A>C