Canonical Allele Identifier: PA165065
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 141306
ClinVar RCV Id: RCV000129775 RCV000484778 RCV000539493 RCV001375560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Glu196Asp
CA013929
NM_001128425.2:c.588G>C
CA340135446
NM_001128425.2:c.588G>T