Canonical Allele Identifier: PA2826827442
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 998698
ClinVar RCV Id: RCV001294588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Val366Leu
CA21835704
NM_001293192.2:c.1096G>C