Canonical Allele Identifier: PA2826826238
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 127833
ClinVar Variation Id: 492024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280120.1:p.Met507Leu
CA011670
NM_001293191.2:c.1519A>T
CA340131758
NM_001293191.2:c.1519A>C