Canonical Allele Identifier: PA2828036468
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1727262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro898Leu
CA16028060
NM_001354904.2:c.2693C>T