Canonical Allele Identifier: PA2828047795
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asp2364Asn
CA013697
NM_001354904.2:c.7090G>A