Canonical Allele Identifier: PA2828042228
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 350413

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Phe1558Leu
CA10618781
NM_001354904.2:c.4672T>C
CA16032379
NM_001354904.2:c.4674T>A
CA16032380
NM_001354904.2:c.4674T>G