Canonical Allele Identifier: PA2827980775
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1716653
ClinVar RCV Id: RCV003743860

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2547Tyr
CA16038105
NM_001354899.2:c.7640C>A