Canonical Allele Identifier: PA2827556632
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_001337579.1:p.Val96Leu
CA340134880
NM_001350650.2:c.286G>T
CA340134881
NM_001350650.2:c.286G>C