Canonical Allele Identifier: PA2741836125
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 2567652
ClinVar RCV Id: RCV003311347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Phe278Ser
CA340134642
NM_001128425.2:c.833T>C