Canonical Allele Identifier: PA2825639613
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser952Asn
CA033901
NM_001127511.3:c.2855G>A