Canonical Allele Identifier: PA2825426504
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 481819
ClinVar RCV Id: RCV000561322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041636.2:p.Ser231Phe
CA340134770
NM_001048171.2:c.692C>T