Canonical Allele Identifier: PA2827966751
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1021385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn1083Lys
CA16028623
NM_001354898.2:c.3249T>A
CA16028624
NM_001354898.2:c.3249T>G