Canonical Allele Identifier: PA916030601
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 182690
ClinVar RCV Id: RCV000160753 RCV000458598 RCV000656909 RCV003987380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.Ala97Val
CA014186
NM_001350651.2:c.290C>T