Canonical Allele Identifier: PA166670
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Val1125Ala
CA008333
NM_001127510.3:c.3374T>C