Canonical Allele Identifier: PA2827971765
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr2601Ala
CA049327
NM_001354898.2:c.7801A>G