Canonical Allele Identifier: PA2827939929
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469975
ClinVar Variation Id: 1499759
ClinVar RCV Id: RCV003745511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asp156Glu
CA039593
NM_001354895.2:c.468C>G
CA16022345
NM_001354895.2:c.468C>A