Canonical Allele Identifier: PA2827557338
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 928029
ClinVar RCV Id: RCV001191678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Thr325Ala
CA340132645
NM_001350650.2:c.973A>G