Canonical Allele Identifier: PA2827994169
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Glu1077Ala
CA10582308
NM_001354901.2:c.3230A>C