Canonical Allele Identifier: PA2828019740
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1022004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asp855Gly
CA035284
NM_001354906.2:c.2564A>G