Canonical Allele Identifier: PA2826826297
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 483902
ClinVar RCV Id: RCV000563136 RCV001037770 RCV001755946
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280120.1:p.Ser526Asn
CA340131538
NM_001293191.2:c.1577G>A