Canonical Allele Identifier: PA916041456
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp2508Asn
CA013697
NM_001354896.2:c.7522G>A