Canonical Allele Identifier: PA2828027503
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1417078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Pro2223Ser
CA046567
NM_001354903.2:c.6667C>T