Canonical Allele Identifier: PA915971112
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 818519
ClinVar RCV Id: RCV001010190
ClinVar Variation Id: 3074808
ClinVar RCV Id: RCV004014342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Asn394Lys
CA340133254
NM_001128425.2:c.1182C>G
CA340133256
NM_001128425.2:c.1182C>A