Canonical Allele Identifier: PA333992
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 188079
ClinVar RCV Id: RCV000167910 RCV000571963 RCV001560234 RCV003320589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Met524Val
CA013059
NM_001128425.2:c.1570A>G