Canonical Allele Identifier: PA2825426913
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 421574
ClinVar RCV Id: RCV000481734

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041636.2:p.Gly368Ser
CA16617156
NM_001048171.2:c.1102G>A