Canonical Allele Identifier: PA2827942618
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 844658
ClinVar RCV Id: RCV003649314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Gly1019Val
CA16028028
NM_001354895.2:c.3056G>T