Canonical Allele Identifier: PA2827989846
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile2532Val
CA013990
NM_001354900.2:c.7594A>G