Canonical Allele Identifier: PA2825432192
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1499605
ClinVar RCV Id: RCV002042384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041639.1:p.Ser507Ala
CA340131617
NM_001048174.1:c.1519T>G