Canonical Allele Identifier: PA2827980584
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2567031
ClinVar RCV Id: RCV003278300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ile2487Leu
CA16037724
NM_001354899.2:c.7459A>C
CA16037725
NM_001354899.2:c.7459A>T