Canonical Allele Identifier: PA2827989930
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr2557Asn
CA049224
NM_001354900.2:c.7670C>A