Canonical Allele Identifier: PA645398950
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428139

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg653Gly
CA16025594
NM_001127510.3:c.1957A>G