Canonical Allele Identifier: PA348957
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220442
ClinVar Variation Id: 470028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp1994Glu
CA043621
NM_001127510.3:c.5982C>G
CA16034426
NM_001127510.3:c.5982C>A