Canonical Allele Identifier: PA2825668130
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1358366
ClinVar RCV Id: RCV001878606
ClinVar Variation Id: 1498998
ClinVar RCV Id: RCV001999437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Trp12Cys
CA089494
NM_001128425.2:c.36G>C
CA340137827
NM_001128425.2:c.36G>T