Canonical Allele Identifier: PA350691
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Val530Ala
CA028518
NM_001127510.3:c.1589T>C