Canonical Allele Identifier: PA2825018242
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1727545
ClinVar RCV Id: RCV002325885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp1033Glu
CA034409
NM_000038.6:c.3099T>A
CA16028121
NM_000038.6:c.3099T>G