Canonical Allele Identifier: PA2825428125
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 862299
ClinVar RCV Id: RCV001068994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041637.1:p.Trp236Ser
CA340134746
NM_001048172.1:c.707G>C