Canonical Allele Identifier: PA2825430939
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 182688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041639.1:p.Trp103Arg
CA013507
NM_001048174.1:c.307T>A
CA340136216
NM_001048174.1:c.307T>C