Canonical Allele Identifier: PA2827967636
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411458

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gln1342His
CA037656
NM_001354898.2:c.4026G>C
CA16030313
NM_001354898.2:c.4026G>T