Canonical Allele Identifier: PA156748
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile2515Val
CA013792
NM_001127510.3:c.7543A>G