Canonical Allele Identifier: PA164269
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 141028
ClinVar RCV Id: RCV000129359 RCV000460472 RCV001731386 RCV001795250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Arg126Gln
CA013471
NM_001128425.2:c.377G>A