Canonical Allele Identifier: PA2825021378
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1395242
ClinVar RCV Id: RCV003772714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr1705Asn
CA16032510
NM_000038.6:c.5114C>A