Canonical Allele Identifier: PA2828019799
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 581688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asp1032Asn
CA16028776
NM_001354903.2:c.3094G>A