Canonical Allele Identifier: PA2827558139
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 464674
ClinVar RCV Id: RCV000532191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.Pro191Leu
CA340133932
NM_001350651.2:c.572C>T