Canonical Allele Identifier: PA2826825192
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 480000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280120.1:p.Glu171Asp
CA340135574
NM_001293191.2:c.513G>C
CA340135578
NM_001293191.2:c.513G>T