Canonical Allele Identifier: PA2825644037
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411542
ClinVar RCV Id: RCV003651892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Leu2383Val
CA16037014
NM_001127511.3:c.7147C>G