Canonical Allele Identifier: PA2828055680
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Val965Ala
CA008333
NM_001354905.2:c.2894T>C