Canonical Allele Identifier: PA2825018143
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1719864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn1017Ser
CA16028012
NM_000038.6:c.3050A>G