Canonical Allele Identifier: PA2828012238
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2773631
ClinVar RCV Id: RCV003584487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro2326Leu
CA16037559
NM_001354905.2:c.6977C>T