Canonical Allele Identifier: PA2827966813
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Val1100Ala
CA008333
NM_001354898.2:c.3299T>C