Canonical Allele Identifier: PA166632
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 141858
ClinVar RCV Id: RCV000130546 RCV000408991 RCV000759155 RCV003987370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Ala419Asp
CA012438
NM_001128425.2:c.1256C>A