Canonical Allele Identifier: PA2825642101
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1692247
ClinVar RCV Id: RCV002257119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro1757Leu
CA16032973
NM_001127511.3:c.5270C>T