Canonical Allele Identifier: PA2827980517
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759129
ClinVar RCV Id: RCV002391535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2469Lys
CA2580072378
NM_001354899.2:c.7405_7406delinsAA