Canonical Allele Identifier: PA2826824701
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 371682
ClinVar RCV Id: RCV000409877 RCV000571651 RCV002505996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280120.1:p.Ala7Val
CA16040740
NM_001293191.2:c.20C>T