Canonical Allele Identifier: PA2825431369
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 492061
ClinVar RCV Id: RCV000581418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041639.1:p.Val242Gly
CA340134688
NM_001048174.1:c.725T>G