Canonical Allele Identifier: PA2828049612
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2628Asn
CA014491
NM_001354904.2:c.7883G>A