Canonical Allele Identifier: PA2828048768
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490365
ClinVar RCV Id: RCV000584490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Phe2494Leu
CA16038407
NM_001354904.2:c.7480T>C
CA16038412
NM_001354904.2:c.7482T>A
CA16038413
NM_001354904.2:c.7482T>G