Canonical Allele Identifier: PA2827959770
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala1763Pro
CA009970
NM_001354897.2:c.5287G>C