Canonical Allele Identifier: PA2827986885
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630006
ClinVar RCV Id: RCV000774872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gly1633Ala
CA16032318
NM_001354900.2:c.4898G>C