Canonical Allele Identifier: PA2825431382
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 449417
ClinVar RCV Id: RCV000519616 RCV000570778 RCV000640346 RCV003159665
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041639.1:p.Arg246Trp
CA059263
NM_001048174.1:c.736C>T
CA645514849
NM_001048174.1:c.735_736delinsTT