Canonical Allele Identifier: PA916018767
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 406850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280125.1:p.Pro82Leu
CA058405
NM_001293196.2:c.245C>T