Canonical Allele Identifier: PA2826827688
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 496102
ClinVar RCV Id: RCV000588717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280124.1:p.Lys14Met
CA340137162
NM_001293195.2:c.41A>T