Canonical Allele Identifier: PA2828029092
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ile2472Val
CA013990
NM_001354903.2:c.7414A>G