Canonical Allele Identifier: PA2827942635
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1727262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Pro1024Leu
CA16028060
NM_001354895.2:c.3071C>T