Canonical Allele Identifier: PA2828047850
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759129
ClinVar RCV Id: RCV002391535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2371Lys
CA2580072378
NM_001354904.2:c.7111_7112delinsAA