Canonical Allele Identifier: PA2825642038
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser1740del
CA041117
NM_001127511.3:c.5218_5220del