Canonical Allele Identifier: PA2828021666
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Pro1175Ser
CA009490
NM_001354906.2:c.3523C>T