Canonical Allele Identifier: PA2580152039
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1718437
ClinVar RCV Id: RCV002299824

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Gln478Leu
CA056389
NM_001128425.2:c.1433A>T