Canonical Allele Identifier: PA916041545
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile2591Val
CA013990
NM_001354896.2:c.7771A>G