Canonical Allele Identifier: PA2827989851
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1716653
ClinVar RCV Id: RCV003743860

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2534Tyr
CA16038105
NM_001354900.2:c.7601C>A