Canonical Allele Identifier: PA168246
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 142402
ClinVar RCV Id: RCV000131501 RCV001062564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Gly337Arg
CA011941
NM_001128425.2:c.1009G>A
CA340133905
NM_001128425.2:c.1009G>C