Canonical Allele Identifier: PA2827558108
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 182695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.Ser181Leu
CA014753
NM_001350651.2:c.542C>T