Canonical Allele Identifier: PA658689361
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490365
ClinVar RCV Id: RCV000584490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Phe2620Leu
CA16038407
NM_001127510.3:c.7858T>C
CA16038412
NM_001127510.3:c.7860T>A
CA16038413
NM_001127510.3:c.7860T>G