Canonical Allele Identifier: PA2828018174
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232412
ClinVar Variation Id: 663857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gly624Arg
CA033124
NM_001354906.2:c.1870G>A
CA033134
NM_001354906.2:c.1870G>C