Canonical Allele Identifier: PA2827944700
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1037892
ClinVar RCV Id: RCV003538713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asp1637Asn
CA16032084
NM_001354895.2:c.4909G>A