Canonical Allele Identifier: PA2825644336
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759129
ClinVar RCV Id: RCV002391535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2479Lys
CA2580072378
NM_001127511.3:c.7435_7436delinsAA