Canonical Allele Identifier: PA2827980725
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927393
ClinVar RCV Id: RCV001190628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Leu2530Val
CA048920
NM_001354899.2:c.7588C>G