Canonical Allele Identifier: PA2827951067
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1021385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn1126Lys
CA16028623
NM_001354896.2:c.3378T>A
CA16028624
NM_001354896.2:c.3378T>G