Canonical Allele Identifier: PA2829726116
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_036354.1:p.Ser222Cys
CA340135286
NM_012222.3:c.665C>G