Canonical Allele Identifier: PA2828047821
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1470437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Leu2367Val
CA16037597
NM_001354904.2:c.7099C>G