Canonical Allele Identifier: PA2827556758
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 141708

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Asn136Lys
CA014451
NM_001350650.2:c.408C>A
CA340134632
NM_001350650.2:c.408C>G