Canonical Allele Identifier: PA2828029634
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 495374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asp2555Gly
CA16038634
NM_001354903.2:c.7664A>G