Canonical Allele Identifier: PA2825636001
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1410428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Val2561Gly
CA16038016
NM_001127510.3:c.7682T>G