Canonical Allele Identifier: PA2825644697
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490365
ClinVar RCV Id: RCV000584490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Phe2602Leu
CA16038407
NM_001127511.3:c.7804T>C
CA16038412
NM_001127511.3:c.7806T>A
CA16038413
NM_001127511.3:c.7806T>G