Canonical Allele Identifier: PA916018695
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 232997
ClinVar RCV Id: RCV000215207 RCV000554382 RCV000766675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280125.1:p.Leu39Met
CA10577734
NM_001293196.2:c.115C>A