Canonical Allele Identifier: PA2828019042
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1727262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Pro923Leu
CA16028060
NM_001354903.2:c.2768C>T