Canonical Allele Identifier: PA163974
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 140942
ClinVar RCV Id: RCV000129217 RCV000226351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Val496Met
CA012933
NM_001128425.2:c.1486G>A