Canonical Allele Identifier: PA2825024471
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759129
ClinVar RCV Id: RCV002391535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2497Lys
CA2580072378
NM_000038.6:c.7489_7490delinsAA