Canonical Allele Identifier: PA2827556895
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 182695
ClinVar RCV Id: RCV000213585 RCV000552627 RCV000766300 RCV001844058
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Ser181Leu
CA014753
NM_001350650.2:c.542C>T