Canonical Allele Identifier: PA2827557778
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 918425
ClinVar RCV Id: RCV001175998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.Pro59Ser
CA340135411
NM_001350651.2:c.175C>T