Canonical Allele Identifier: PA916030602
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 406859
ClinVar RCV Id: RCV000468855 RCV000565823 RCV001356323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.Ala97Thr
CA058824
NM_001350651.2:c.289G>A