Canonical Allele Identifier: PA2828019202
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asp775Gly
CA008117
NM_001354906.2:c.2324A>G