Canonical Allele Identifier: PA2826828587
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 142402
ClinVar RCV Id: RCV000131501 RCV001062564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280124.1:p.Gly309Arg
CA011941
NM_001293195.2:c.925G>A
CA340133905
NM_001293195.2:c.925G>C