Canonical Allele Identifier: PA2825642477
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn1885Ser
CA042707
NM_001127511.3:c.5654A>G