Canonical Allele Identifier: PA2827968360
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1369536
ClinVar RCV Id: RCV001870683

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr1560Ala
CA16031754
NM_001354898.2:c.4678A>G