Canonical Allele Identifier: PA2827947089
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Pro2369Ser
CA046951
NM_001354895.2:c.7105C>T