Canonical Allele Identifier: PA2825023810
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1417078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro2324Ser
CA046567
NM_000038.6:c.6970C>T