Canonical Allele Identifier: PA2827966509
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 923028
ClinVar RCV Id: RCV001183414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly1014Ala
CA16028162
NM_001354898.2:c.3041G>C