Canonical Allele Identifier: PA2827990641
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr2772Lys
CA16039637
NM_001354900.2:c.8315C>A