Canonical Allele Identifier: PA2827558029
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 571385
ClinVar RCV Id: RCV000692520 RCV001018522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.Ser155Arg
CA21837059
NM_001350651.2:c.465C>G
CA340134424
NM_001350651.2:c.465C>A
CA340134431
NM_001350651.2:c.463A>C