Canonical Allele Identifier: PA2828012334
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759129
ClinVar RCV Id: RCV002391535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2337Lys
CA2580072378
NM_001354905.2:c.7009_7010delinsAA