Canonical Allele Identifier: PA299557
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 182691
ClinVar RCV Id: RCV000160754 RCV000191933 RCV000221854 RCV003162678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Gly286Glu
CA014470
NM_001128425.2:c.857G>A