Canonical Allele Identifier: PA2827948379
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser2754Asn
CA014491
NM_001354895.2:c.8261G>A