Canonical Allele Identifier: PA2828009385
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asp1876Asn
CA16034696
NM_001354905.2:c.5626G>A