Canonical Allele Identifier: PA916039934
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482506

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gly895Ala
CA032861
NM_001354896.2:c.2684G>C