Canonical Allele Identifier: PA2825024833
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1692385
ClinVar RCV Id: RCV002257179

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2594Ala
CA16038234
NM_000038.6:c.7780T>G