Canonical Allele Identifier: PA915971214
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 818803
ClinVar RCV Id: RCV001010762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Gly429Arg
CA340132894
NM_001128425.2:c.1285G>C
CA340132895
NM_001128425.2:c.1285G>A