Canonical Allele Identifier: PA2827999222
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn2609del
CA2580072453
NM_001354901.2:c.7824_7826del