Canonical Allele Identifier: PA2827998095
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1417078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro2265Ser
CA046567
NM_001354901.2:c.6793C>T