Canonical Allele Identifier: PA2827970909
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 571390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr2342Ala
CA046911
NM_001354898.2:c.7024A>G