Canonical Allele Identifier: PA2826829188
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41756
ClinVar RCV Id: RCV000034673 RCV000121603 RCV000115762 RCV000144641 RCV000986299 RCV002490462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280124.1:p.Leu501Met
CA011679
NM_001293195.2:c.1501C>A