Canonical Allele Identifier: PA2825432021
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1772772
ClinVar RCV Id: RCV002394428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041639.1:p.His454Tyr
CA340132562
NM_001048174.1:c.1360C>T