Canonical Allele Identifier: PA2828013339
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 433679
ClinVar RCV Id: RCV000502714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asp2496Tyr
CA16038632
NM_001354905.2:c.7486G>T