Canonical Allele Identifier: PA658659124
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.His307Tyr
CA16023323
NM_001127510.3:c.919C>T