Canonical Allele Identifier: PA2827947083
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 571390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Thr2367Ala
CA046911
NM_001354895.2:c.7099A>G