Canonical Allele Identifier: PA2827988503
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Pro2129Ser
CA16035571
NM_001354900.2:c.6385C>T