Canonical Allele Identifier: PA2825641720
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1744419
ClinVar RCV Id: RCV002342801

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala1636Gly
CA16032195
NM_001127511.3:c.4907C>G