Canonical Allele Identifier: PA2825642748
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro1968Leu
CA043504
NM_001127511.3:c.5903C>T