Canonical Allele Identifier: PA915971458
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 801227
ClinVar RCV Id: RCV000985855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Met506Val
CA340132302
NM_001128425.2:c.1516A>G