Canonical Allele Identifier: PA2825428690
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1018594
ClinVar RCV Id: RCV001317921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041637.1:p.His421Tyr
CA340132773
NM_001048172.1:c.1261C>T