Canonical Allele Identifier: PA658681778
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469796
ClinVar RCV Id: RCV003742636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Leu22Phe
CA360611829
NM_001127511.3:c.64C>T