Canonical Allele Identifier: PA2827989967
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr2570Lys
CA049276
NM_001354900.2:c.7709C>A