Canonical Allele Identifier: PA2827943020
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629986
ClinVar RCV Id: RCV000774851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asp1134Gly
CA16028788
NM_001354895.2:c.3401A>G