Canonical Allele Identifier: PA2827998477
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 971797
ClinVar RCV Id: RCV003652111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Phe2384Leu
CA16037285
NM_001354901.2:c.7150T>C
CA16037290
NM_001354901.2:c.7152C>A
CA16037291
NM_001354901.2:c.7152C>G