Canonical Allele Identifier: PA2827990141
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1932430
ClinVar RCV Id: RCV002605780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Glu2621Val
CA16038674
NM_001354900.2:c.7862A>T