Canonical Allele Identifier: PA658671951
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 483899
ClinVar RCV Id: RCV000567165

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Gln425His
CA340132910
NM_001128425.2:c.1275G>T
CA340132911
NM_001128425.2:c.1275G>C