Canonical Allele Identifier: PA2827980722
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2586992
ClinVar RCV Id: RCV003341968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2529Ala
CA16037992
NM_001354899.2:c.7585T>G