Canonical Allele Identifier: PA2825636453
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1332383
ClinVar RCV Id: RCV001805429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr1773Pro
CA16032957
NM_001127510.3:c.5317A>C