Canonical Allele Identifier: PA2826828239
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1005897
ClinVar RCV Id: RCV001302848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280124.1:p.Ser197Cys
CA340135286
NM_001293195.2:c.590C>G