Canonical Allele Identifier: PA2826829586
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 141708

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280125.1:p.Asn159Lys
CA014451
NM_001293196.2:c.477C>A
CA340134632
NM_001293196.2:c.477C>G