Canonical Allele Identifier: PA2827986937
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 419787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Pro1650Thr
CA16032418
NM_001354900.2:c.4948C>A