Canonical Allele Identifier: PA2827962283
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1059095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp2529Gly
CA16037756
NM_001354897.2:c.7586A>G