Canonical Allele Identifier: PA2826827007
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 134862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Ser226Leu
CA012017
NM_001293192.2:c.677C>T