Canonical Allele Identifier: PA2827971767
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr2601Ile
CA014137
NM_001354898.2:c.7802C>T