Canonical Allele Identifier: PA2825022654
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp2036Asn
CA16034696
NM_000038.6:c.6106G>A