Canonical Allele Identifier: PA191776
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 185383
ClinVar RCV Id: RCV000164793 RCV000659899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.His448Asp
CA012643
NM_001128425.2:c.1342C>G