Canonical Allele Identifier: PA2827953333
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760417
ClinVar RCV Id: RCV002400793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Glu2600Asp
CA16038154
NM_001354896.2:c.7800A>C
CA16038155
NM_001354896.2:c.7800A>T