Canonical Allele Identifier: PA2827990456
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2713Asn
CA014491
NM_001354900.2:c.8138G>A