Canonical Allele Identifier: PA2827557199
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 2061307
ClinVar RCV Id: RCV002942622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Trp284Cys
CA340132901
NM_001350650.2:c.852G>T
CA340132902
NM_001350650.2:c.852G>C