Canonical Allele Identifier: PA2825645030
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Leu2704Pro
CA050043
NM_001127511.3:c.8111T>C