Canonical Allele Identifier: PA2827967679
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr1355Ile
CA10578369
NM_001354898.2:c.4064C>T