Canonical Allele Identifier: PA916042483
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_001341834.1:p.Asp97Glu
CA039593
NM_001354905.2:c.291C>G
CA16022345
NM_001354905.2:c.291C>A