Canonical Allele Identifier: PA16040139
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr2598Asn
CA049224
NM_000038.6:c.7793C>A