Canonical Allele Identifier: PA166192
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 141708
ClinVar RCV Id: RCV000130325 RCV001232259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Asn279Lys
CA014451
NM_001128425.2:c.837C>A
CA340134632
NM_001128425.2:c.837C>G