Canonical Allele Identifier: PA2828019528
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ala824Ser
CA16028614
NM_001354906.2:c.2470G>T