Canonical Allele Identifier: PA2828023799
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 486773

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gln1651Leu
CA16032826
NM_001354903.2:c.4952A>T