Canonical Allele Identifier: PA2827999019
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2755712
ClinVar RCV Id: RCV003536843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Val2547Glu
CA16038315
NM_001354901.2:c.7640T>A