Canonical Allele Identifier: PA2825644402
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1059095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asp2501Gly
CA16037756
NM_001127511.3:c.7502A>G