Canonical Allele Identifier: PA117386
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 5294
ClinVar RCV Id: RCV000005614 RCV000005615 RCV000079501 RCV000115748 RCV000121598 RCV000144637 RCV000493920 RCV000515320 RCV000477907 RCV000501239 RCV001262769 RCV001574076 RCV001580144 RCV002051775 RCV004528084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Gly396Asp
CA011561
NM_001128425.2:c.1187G>A