Canonical Allele Identifier: PA658803736
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn1118Ser
CA16028677
NM_001127510.3:c.3353A>G