Canonical Allele Identifier: PA2825636863
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1492941
ClinVar RCV Id: RCV003773254

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Trp25Ser
CA360611861
NM_001127511.3:c.74G>C