Canonical Allele Identifier: PA645453900
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 216871
ClinVar RCV Id: RCV000199700 RCV000223299
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Gln500_Gln501delinsCysTrp
CA338806
NM_001128425.2:c.1498_1502delinsTGTTG