Canonical Allele Identifier: PA2827971661
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760562
ClinVar RCV Id: RCV002409781

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Val2567Gly
CA16038224
NM_001354898.2:c.7700T>G