Canonical Allele Identifier: PA2827971312
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 657079

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Leu2463Arg
CA16037570
NM_001354898.2:c.7388T>G