Canonical Allele Identifier: PA2827980759
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760274
ClinVar RCV Id: RCV002400650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2543Tyr
CA16038083
NM_001354899.2:c.7628C>A