Canonical Allele Identifier: PA2827947434
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 229765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Pro2471Leu
CA10578443
NM_001354895.2:c.7412C>T