Canonical Allele Identifier: PA2828025356
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Pro1885Leu
CA043504
NM_001354903.2:c.5654C>T