Canonical Allele Identifier: PA2828027827
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132747

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn2119Tyr
CA012931
NM_001354906.2:c.6355A>T