Canonical Allele Identifier: PA2825629708
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1009641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp1022Gly
CA16028046
NM_001127510.3:c.3065A>G