Canonical Allele Identifier: PA2827950914
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp1076Gly
CA008117
NM_001354896.2:c.3227A>G