Canonical Allele Identifier: PA916030598
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 372416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.Asn95Ser
CA16042398
NM_001350651.2:c.284A>G