Canonical Allele Identifier: PA2827999069
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro2563Thr
CA16038419
NM_001354901.2:c.7687C>A