Canonical Allele Identifier: PA2827998209
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2587029
ClinVar RCV Id: RCV003339110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2302Pro
CA16036756
NM_001354901.2:c.6904T>C