Canonical Allele Identifier: PA2825432020
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1772769
ClinVar RCV Id: RCV002394425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041639.1:p.His454Asp
CA340132563
NM_001048174.1:c.1360C>G