Canonical Allele Identifier: PA2827943035
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2054609
ClinVar RCV Id: RCV003744812

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asp1138Asn
CA16028812
NM_001354895.2:c.3412G>A