Canonical Allele Identifier: PA2827945995
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asp2033Glu
CA010908
NM_001354895.2:c.6099C>G
CA16034682
NM_001354895.2:c.6099C>A