Canonical Allele Identifier: PA658660296
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp2036Asn
CA16034696
NM_001127510.3:c.6106G>A