Canonical Allele Identifier: PA2825021317
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr1692Arg
CA16032428
NM_000038.6:c.5075C>G