Canonical Allele Identifier: PA2827962210
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759129
ClinVar RCV Id: RCV002391535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2507Lys
CA2580072378
NM_001354897.2:c.7519_7520delinsAA