Canonical Allele Identifier: PA168180
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 142369
ClinVar RCV Id: RCV000131452 RCV000824066 RCV001194163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Asn42Ser
CA012458
NM_001128425.2:c.125A>G