Canonical Allele Identifier: PA166520
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 135983
ClinVar RCV Id: RCV000123142 RCV000130485 RCV000515285 RCV000590647 RCV001175350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Ala419Thr
CA012424
NM_001128425.2:c.1255G>A