Canonical Allele Identifier: PA2825021567
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 486773

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gln1752Leu
CA16032826
NM_000038.6:c.5255A>T