Canonical Allele Identifier: PA2827942959
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asn1118Ser
CA16028677
NM_001354895.2:c.3353A>G