Canonical Allele Identifier: PA2827968949
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141021

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gln1739Glu
CA010025
NM_001354898.2:c.5215C>G