Canonical Allele Identifier: PA2825637681
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Leu286Pro
CA16023306
NM_001127511.3:c.857T>C