Canonical Allele Identifier: PA2825016062
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428139

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg653Gly
CA16025594
NM_000038.6:c.1957A>G