Canonical Allele Identifier: PA2827957675
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Val1135Ala
CA008333
NM_001354897.2:c.3404T>C