Canonical Allele Identifier: PA2828018999
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asp917Asn
CA008010
NM_001354903.2:c.2749G>A