Canonical Allele Identifier: PA2825426929
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 662771
ClinVar RCV Id: RCV000820500
ClinVar Variation Id: 818576

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041636.2:p.Glu375Asp
CA340133116
NM_001048171.2:c.1125G>T
CA340133119
NM_001048171.2:c.1125G>C