Canonical Allele Identifier: PA2827999521
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2695Asn
CA014491
NM_001354901.2:c.8084G>A