Canonical Allele Identifier: PA2827969204
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro1818Leu
CA010490
NM_001354898.2:c.5453C>T