Canonical Allele Identifier: PA2827957304
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp1028Asn
CA008010
NM_001354897.2:c.3082G>A