Canonical Allele Identifier: PA16040138
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Lys2585Thr
CA10578450
NM_000038.6:c.7754A>C