Canonical Allele Identifier: PA2826829765
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41767
ClinVar RCV Id: RCV000034684 RCV000079500 RCV000131427 RCV000144634 RCV000299432 RCV001270291
ClinVar Variation Id: 492713
ClinVar RCV Id: RCV000584255 RCV000640420 RCV000777602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280125.1:p.Gln218His
CA011883
NM_001293196.2:c.654G>C
CA340133885
NM_001293196.2:c.654G>T