Canonical Allele Identifier: PA2828018993
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 438873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Tyr744Asp
CA16028076
NM_001354906.2:c.2230T>G