Canonical Allele Identifier: PA2827962535
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2676989
ClinVar RCV Id: RCV003463101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile2605Leu
CA16038237
NM_001354897.2:c.7813A>C