Canonical Allele Identifier: PA2829726632
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 421574
ClinVar RCV Id: RCV000481734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036354.1:p.Gly393Ser
CA16617156
NM_012222.3:c.1177G>A