Canonical Allele Identifier: PA2825668730
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 3073893
ClinVar RCV Id: RCV004012435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Ser515Tyr
CA340131871
NM_001128425.2:c.1544C>A