Canonical Allele Identifier: PA2827558735
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 127833
ClinVar Variation Id: 492024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.Met381Leu
CA011670
NM_001350651.2:c.1141A>T
CA340131758
NM_001350651.2:c.1141A>C