Canonical Allele Identifier: PA2827998565
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 757607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2410del
CA915943521
NM_001354901.2:c.7227_7229del