Canonical Allele Identifier: PA2827556710
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 862299
ClinVar RCV Id: RCV001068994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Trp120Ser
CA340134746
NM_001350650.2:c.359G>C