Canonical Allele Identifier: PA192399
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 185604
ClinVar RCV Id: RCV000165052 RCV000466109 RCV000590403 RCV001731494 RCV002478507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Val132Ile
CA013526
NM_001128425.2:c.394G>A