Canonical Allele Identifier: PA2827971555
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760090
ClinVar RCV Id: RCV002400466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro2534Leu
CA16038006
NM_001354898.2:c.7601C>T