Canonical Allele Identifier: PA2827971602
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1716653
ClinVar RCV Id: RCV003743860

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2550Tyr
CA16038105
NM_001354898.2:c.7649C>A