Canonical Allele Identifier: PA916041532
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 628704
ClinVar RCV Id: RCV000773365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2570Gly
CA16037959
NM_001354896.2:c.7708A>G