Canonical Allele Identifier: PA2827942617
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1799283
ClinVar RCV Id: RCV002444130

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asp1018Ala
CA16028018
NM_001354895.2:c.3053A>C