Canonical Allele Identifier: PA2825024696
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927393
ClinVar RCV Id: RCV001190628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Leu2558Val
CA048920
NM_000038.6:c.7672C>G