Canonical Allele Identifier: PA198135
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 187628
ClinVar RCV Id: RCV000167374 RCV000409405 RCV000993997 RCV003226228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Val239Ile
CA014175
NM_001128425.2:c.715G>A