Canonical Allele Identifier: PA2827971742
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490365
ClinVar RCV Id: RCV000584490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Phe2595Leu
CA16038407
NM_001354898.2:c.7783T>C
CA16038412
NM_001354898.2:c.7785T>A
CA16038413
NM_001354898.2:c.7785T>G