Canonical Allele Identifier: PA916018692
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 185653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280125.1:p.Pro37Leu
CA013620
NM_001293196.2:c.110C>T