Canonical Allele Identifier: PA2827966492
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482450

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp1008Tyr
CA16028117
NM_001354898.2:c.3022G>T