Canonical Allele Identifier: PA2827971870
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 495374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp2631Gly
CA16038634
NM_001354898.2:c.7892A>G