Canonical Allele Identifier: PA2825639730
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1039704

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Glu1002Ala
CA16028032
NM_001127511.3:c.3005A>C