Canonical Allele Identifier: PA916041597
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490365
ClinVar RCV Id: RCV000584490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Phe2638Leu
CA16038407
NM_001354896.2:c.7912T>C
CA16038412
NM_001354896.2:c.7914T>A
CA16038413
NM_001354896.2:c.7914T>G