Canonical Allele Identifier: PA2825431982
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 142894
ClinVar RCV Id: RCV000132362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041639.1:p.Pro442Ala
CA012704
NM_001048174.1:c.1324C>G