Canonical Allele Identifier: PA2826827570
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 127833
ClinVar Variation Id: 492024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Met404Leu
CA011670
NM_001293192.2:c.1210A>T
CA340131758
NM_001293192.2:c.1210A>C