Canonical Allele Identifier: PA916041133
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181815

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.His2250Asp
CA012407
NM_001354896.2:c.6748C>G