Canonical Allele Identifier: PA2825024853
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 859980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gln2600Glu
CA16038267
NM_000038.6:c.7798C>G