Canonical Allele Identifier: PA2827946853
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser2296Asn
CA16036358
NM_001354895.2:c.6887G>A