Canonical Allele Identifier: PA2828034252
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ala571Val
CA030702
NM_001354904.2:c.1712C>T