Canonical Allele Identifier: PA2827556971
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 926218
ClinVar Variation Id: 2111333
ClinVar RCV Id: RCV003023932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Asp207Glu
CA060205
NM_001350650.2:c.621C>A
CA340133753
NM_001350650.2:c.621C>G