Canonical Allele Identifier: PA2825024820
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 946681
ClinVar RCV Id: RCV003538615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.His2591Arg
CA16038215
NM_000038.6:c.7772A>G