Canonical Allele Identifier: PA2828004260
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.His2500Asp
CA16038213
NM_001354902.2:c.7498C>G