Canonical Allele Identifier: PA2827987156
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 486773

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gln1711Leu
CA16032826
NM_001354900.2:c.5132A>T