Canonical Allele Identifier: PA2828049032
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489501
ClinVar RCV Id: RCV000580553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asp2530Asn
CA16038630
NM_001354904.2:c.7588G>A