Canonical Allele Identifier: PA916041297
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Lys2375Glu
CA16036732
NM_001354896.2:c.7123A>G