Canonical Allele Identifier: PA2828002852
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg1651Leu
CA16032754
NM_001354902.2:c.4952G>T