Canonical Allele Identifier: PA215827
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41752
ClinVar RCV Id: RCV000034669 RCV000115755 RCV000123143 RCV000212714 RCV001353918 RCV004528162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Leu420Met
CA011605
NM_001128425.2:c.1258C>A