Canonical Allele Identifier: PA916018664
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 406831
ClinVar RCV Id: RCV000467752 RCV003168772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280124.1:p.Arg5Gly
CA056632
NM_001293195.2:c.13C>G