Canonical Allele Identifier: PA2826826351
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 182688
ClinVar RCV Id: RCV000160751 RCV000212700 RCV000701601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Trp11Arg
CA013507
NM_001293192.2:c.31T>A
CA340136216
NM_001293192.2:c.31T>C