Canonical Allele Identifier: PA16040120
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 229765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro2471Leu
CA10578443
NM_000038.6:c.7412C>T