Canonical Allele Identifier: PA2827998210
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3231145
ClinVar RCV Id: RCV004525216

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Gly2303Val
CA046822
NM_001354901.2:c.6908G>T