Canonical Allele Identifier: PA645400197
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg1676del
CA3368170
NM_001127510.3:c.5026_5028del