Canonical Allele Identifier: PA2827556708
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 3233052
ClinVar RCV Id: RCV004523684

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Leu119Phe
CA340134753
NM_001350650.2:c.355C>T