Canonical Allele Identifier: PA2825430156
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 5298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041638.1:p.Pro377Ser
CA011572
NM_001048173.1:c.1129C>T