Canonical Allele Identifier: PA2825644491
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 628704
ClinVar RCV Id: RCV000773365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2534Gly
CA16037959
NM_001127511.3:c.7600A>G