Canonical Allele Identifier: PA2828028405
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 229765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Pro2370Leu
CA10578443
NM_001354903.2:c.7109C>T