Canonical Allele Identifier: PA2826823707
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 483915
ClinVar RCV Id: RCV000565067
ClinVar Variation Id: 2119286
ClinVar RCV Id: RCV003054583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280119.1:p.Val226Leu
CA340134880
NM_001293190.2:c.676G>T
CA340134881
NM_001293190.2:c.676G>C