Canonical Allele Identifier: PA145641
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gly2484Ser
CA013731
NM_001127511.3:c.7450G>A