Canonical Allele Identifier: PA2827558209
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 406827
ClinVar RCV Id: RCV000474007 RCV000574563 RCV000481886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.Pro216Leu
CA16610177
NM_001350651.2:c.647C>T