Canonical Allele Identifier: PA2828029098
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760562
ClinVar RCV Id: RCV002409781

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Val2309Gly
CA16038224
NM_001354906.2:c.6926T>G