Canonical Allele Identifier: PA2827980403
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236643

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2436Tyr
CA047889
NM_001354899.2:c.7307C>A