Canonical Allele Identifier: PA2828022958
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 183069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asp1535Tyr
CA009798
NM_001354903.2:c.4603G>T