Canonical Allele Identifier: PA2825639771
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1727545
ClinVar RCV Id: RCV002325885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asp1015Glu
CA034409
NM_001127511.3:c.3045T>A
CA16028121
NM_001127511.3:c.3045T>G