Canonical Allele Identifier: PA2828001394
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1039704

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Glu929Ala
CA16028032
NM_001354902.2:c.2786A>C