Canonical Allele Identifier: PA658804267
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 533317
ClinVar RCV Id: RCV000640390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Leu460Ser
CA340132694
NM_001128425.2:c.1379T>C