Canonical Allele Identifier: PA2828028600
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759129
ClinVar RCV Id: RCV002391535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2396Lys
CA2580072378
NM_001354903.2:c.7186_7187delinsAA