Canonical Allele Identifier: PA2827985064
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Val1084Ala
CA008333
NM_001354900.2:c.3251T>C