Canonical Allele Identifier: PA2827981796
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489432

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Tyr37Cys
CA033841
NM_001354900.2:c.110A>G