Canonical Allele Identifier: PA915971297
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 819017
ClinVar RCV Id: RCV001011196 RCV004004497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Tyr456Cys
CA340132718
NM_001128425.2:c.1367A>G