Canonical Allele Identifier: PA2828004263
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 628605
ClinVar RCV Id: RCV000773146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.His2500Tyr
CA16038214
NM_001354902.2:c.7498C>T