Canonical Allele Identifier: PA2825641859
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 234162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala1682Val
CA10578393
NM_001127511.3:c.5045C>T