Canonical Allele Identifier: PA2827971747
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 75619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro2597Leu
CA16038424
NM_001354898.2:c.7790C>T