Canonical Allele Identifier: PA2827999029
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 957922
ClinVar RCV Id: RCV003650807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Gly2551Ala
CA16038341
NM_001354901.2:c.7652G>C