Canonical Allele Identifier: PA338912
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 216520
ClinVar RCV Id: RCV000199845 RCV000216921 RCV000502616 RCV001589079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Ala13Thr
CA338910
NM_001128425.2:c.37G>A