Canonical Allele Identifier: PA2828002868
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 486773

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gln1661Leu
CA16032826
NM_001354902.2:c.4982A>T