Canonical Allele Identifier: PA2826826777
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 481792
ClinVar RCV Id: RCV000567883 RCV002528009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Val150Leu
CA340134691
NM_001293192.2:c.448G>T
CA340134692
NM_001293192.2:c.448G>C