Canonical Allele Identifier: PA2827999227
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 801042
ClinVar RCV Id: RCV000985323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro2610Thr
CA16038721
NM_001354901.2:c.7828C>A