Canonical Allele Identifier: PA2825636979
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1380202
ClinVar RCV Id: RCV002552311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala51Pro
CA360612174
NM_001127511.3:c.151G>C