Canonical Allele Identifier: PA2828001411
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2122352
ClinVar RCV Id: RCV003744979

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Leu938Arg
CA16028093
NM_001354902.2:c.2813T>G