Canonical Allele Identifier: PA2827989639
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 433676

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Pro2468Ser
CA16037691
NM_001354900.2:c.7402C>T