Canonical Allele Identifier: PA2828050665
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489432

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Tyr37Cys
CA033841
NM_001354905.2:c.110A>G