Canonical Allele Identifier: PA2827971366
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1511850
ClinVar RCV Id: RCV003773417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ala2476Ser
CA16037645
NM_001354898.2:c.7426G>T