Canonical Allele Identifier: PA2827979631
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181815

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.His2204Asp
CA012407
NM_001354899.2:c.6610C>G