Canonical Allele Identifier: PA2828028478
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759129
ClinVar RCV Id: RCV002391535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2214Lys
CA2580072378
NM_001354906.2:c.6640_6641delinsAA