Canonical Allele Identifier: PA2827557629
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 629132
ClinVar RCV Id: RCV000773822
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.Trp13Arg
CA340136023
NM_001350651.2:c.37T>C
CA340136025
NM_001350651.2:c.37T>A