Canonical Allele Identifier: PA189698
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile2573Val
CA013990
NM_001127510.3:c.7717A>G