Canonical Allele Identifier: PA2828041755
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1037892
ClinVar RCV Id: RCV003538713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asp1511Asn
CA16032084
NM_001354904.2:c.4531G>A