Canonical Allele Identifier: PA658689366
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro2622Thr
CA16038419
NM_001127510.3:c.7864C>A